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. 2020 May 7;11(5):327. doi: 10.1038/s41419-020-2510-4

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© The Author(s) 2020

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 4 — a Western blot assay for CK1δ and β-TRCP proteins in hucMSC-Ex (n = 4). b The internalization of hucMSC-Ex (PKH67, green) in NRK-52E cells was observed by confocal microscopy. Bar = 25 μm. c The expression of CK1δ and β-TRCP in NRK-52E cells under mechanical stress. Bar = 25 μm. d The expression of CK1δ, β-TRCP, and YAP in the kidneys of 14d UUO rats with hucMSC-Ex treatment was determined by immunohistochemistry. Bar = 100 μm. e Western blot assay for CK1δ and β-TRCP proteins in the kidneys of 14d UUO rats treated with hucMSC-Ex (n = 3). f NRK-52E cells were pre-treated with MG132 (20 μm) for 5 h followed by stiff gel stimulation in the presence of hucMSC-Ex. YAP protein level was detected by western blot. g The ubiquitination of YAP protein with hucMSC-Ex treatment determined by co-IP.